Canonical Allele Identifier: PA2827663781
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 218248
ClinVar RCV Id: RCV000235343

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339535.1:p.Asp95Gly
CA10575823
NM_001352606.2:c.284A>G